{
  "id": 25078,
  "label": "variable-age onset combined generalized and focal epilepsy syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800494",
  "properties": {
    "xrefs": [
      "GARD:0027393"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An epilepsy syndrome characterized by a combined generalized and focal epilepsy syndromes where age at seizure onset varies."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 24297,
      "label": "combined generalized and focal epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7064,
        24298
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1836943",
          "UMLS:C5816884"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any epilepsy where patients have both generalized and focal seizure types, with interictal and/or ictal EEG findings that accompany both seizure types. Patients with Dravet syndrome and Lennox-Gastaut syndrome may have combined focal and generalized epilepsy."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100573"
    },
    {
      "id": 24339,
      "label": "variable age epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027372",
          "Orphanet:699645"
        ],
        "synonyms": [
          "variable age onset epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome that has an onset during variable ages and stages of life."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100619"
    }
  ],
  "children": [
    {
      "id": 8940,
      "label": "reading seizures",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17993,
        25078
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017029",
          "MEDGEN:75817",
          "OMIM:132300",
          "Orphanet:166433",
          "UMLS:C0278193"
        ],
        "synonyms": [
          "EwRIS",
          "epilepsy with reading-induced seizures",
          "epilepsy, reading"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare reflex epilepsy characterized by reading-induced seizures which in most cases present with orofacial/jaw myoclonus possibly extending to the upper limbs but can also manifest as dyslexia or alexia and visual symptoms. In both variants secondary generalized tonic-clonic seizures may evolve if the stimulus is not interrupted. The disease typically begins in the second or third decade of life and may be inherited in an autosomal dominant pattern. It usually takes a benign course with little tendency to spontaneous seizures."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007560"
    }
  ],
  "roots": [
    {
      "id": 24297,
      "label": "combined generalized and focal epilepsy"
    },
    {
      "id": 24339,
      "label": "variable age epilepsy syndrome"
    }
  ]
}